Medical Device Manufacturer · US , Minnesota , MN

Interacoustics A/S - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 2006

Total

Cleared

Denied

Interacoustics A/S has 17 FDA 510(k) cleared medical devices. Based in Minnesota, US.

Historical record: 17 cleared submissions from 2006 to 2020. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Interacoustics A/S Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Interacoustics A/S

17 devices

1-17 of 17

Cleared Aug 12, 2020

Orion

K200529 · LXV

Ear, Nose, Throat · 163d

Cleared Aug 12, 2020

VisualEyes

K200534 · GWN

Ear, Nose, Throat · 163d

Cleared May 27, 2020

TRV

K192652 · LXV

Ear, Nose, Throat · 246d

Cleared Jul 15, 2019

Lyra

K191372 · EWO

Ear, Nose, Throat · 54d

Cleared Feb 14, 2018

Sera

K173567 · EWO

Ear, Nose, Throat · 86d

Ear, Nose, Throat · 30d

Ear, Nose, Throat · 90d

Cleared Nov 29, 2012

TITAN

K121847 · ETY

Ear, Nose, Throat · 157d

Ear, Nose, Throat · 125d

Cleared Feb 05, 2008

VN415M, VN415B, VO425M, V0425B, 2D-VOG GOGGLES, 2D-VOG SYSTEM

K072254 · GWN

Neurology · 175d

Cleared Jun 29, 2007

INTERACOUSTICS ASSR, ECLIPSE SYSTEM (CABINET NAME)

K070696 · GWJ

Neurology · 108d

Cleared Jun 23, 2006

PILOT TEST OR DETECTIVE AUDIOMETERS

K060883 · EWO

Ear, Nose, Throat · 84d

Interacoustics A/S - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Interacoustics A/S

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